Canonical Allele Identifier: CA2570018217
Gene: FLVCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883639_212883640insAAAT , CM000663.2:g.212883639_212883640insAAAT GRCh38
NC_000001.10:g.213056981_213056982insAAAT , CM000663.1:g.213056981_213056982insAAAT GRCh37
NC_000001.9:g.211123604_211123605insAAAT NCBI36
NG_028131.1:g.30385_30386insAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1092+201_1092+202insAAAT MANE Select ENSP00000355938.4:n.1092+201_1092+202insAAAT
ENST00000366971.8:c.1092+201_1092+202insAAAT ENSP00000355938.4:n.1092+201_1092+202insAAAT
ENST00000419102.1:c.488+201_488+202insAAAT
ENST00000474693.1:n.317+201_317+202insAAAT
ENST00000483790.1:n.30+201_30+202insAAAT
NM_014053.3:c.1092+201_1092+202insAAAT NP_054772.1:n.1092+201_1092+202insAAAT
XM_011509446.1:c.1092+201_1092+202insAAAT XP_011507748.1:n.1092+201_1092+202insAAAT
XR_247024.1:n.1266+201_1266+202insAAAT
XR_426771.1:n.1393+201_1393+202insAAAT
XM_011509446.3:c.1092+201_1092+202insAAAT XP_011507748.1:n.1092+201_1092+202insAAAT
XR_247024.3:n.1266+201_1266+202insAAAT
NM_014053.4:c.1092+201_1092+202insAAAT MANE Select NP_054772.1:n.1092+201_1092+202insAAAT